Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs964184 | 0.716 | 0.440 | 11 | 116778201 | 3 prime UTR variant | G/C | snv | 0.82 | 47 | ||
rs115849089 | 8 | 20054859 | intergenic variant | G/A | snv | 9.8E-02 | 7 | ||||
rs150641967 | 19 | 19259532 | intron variant | AGAC/-;AGACAGAC | delins | 4 | |||||
rs11667159 | 19 | 46291989 | intergenic variant | C/A;T | snv | 3 | |||||
rs11668290 | 19 | 46292921 | upstream gene variant | G/A | snv | 0.12 | 3 | ||||
rs11671319 | 19 | 46291810 | intergenic variant | T/C | snv | 0.12 | 3 | ||||
rs11671360 | 19 | 46291914 | intergenic variant | T/C | snv | 0.12 | 3 | ||||
rs11671710 | 19 | 46288677 | regulatory region variant | C/G;T | snv | 3 | |||||
rs117366905 | 19 | 46294033 | upstream gene variant | A/G | snv | 0.12 | 3 | ||||
rs117992292 | 19 | 46294038 | upstream gene variant | A/G | snv | 0.12 | 3 | ||||
rs141332218 | 19 | 46293976 | upstream gene variant | T/C | snv | 0.12 | 3 | ||||
rs142815467 | 19 | 46291277 | intergenic variant | -/T | delins | 0.12 | 3 | ||||
rs34128150 | 19 | 46291852 | intergenic variant | C/A | snv | 0.12 | 3 | ||||
rs7254961 | 19 | 46292627 | upstream gene variant | C/T | snv | 0.12 | 3 | ||||
rs7256047 | 19 | 46292776 | upstream gene variant | T/C | snv | 0.12 | 3 | ||||
rs73059722 | 19 | 46293161 | upstream gene variant | G/A | snv | 0.12 | 3 | ||||
rs73059723 | 19 | 46293245 | upstream gene variant | A/C | snv | 0.12 | 3 | ||||
rs73059724 | 19 | 46293510 | upstream gene variant | T/C | snv | 0.11 | 3 | ||||
rs73059725 | 19 | 46293511 | upstream gene variant | G/A | snv | 0.11 | 3 | ||||
rs73059726 | 19 | 46293937 | upstream gene variant | G/A | snv | 0.12 | 3 | ||||
rs80095739 | 19 | 46282441 | regulatory region variant | A/G | snv | 0.10 | 3 | ||||
rs145556679 | 11 | 117772549 | intron variant | G/A;C | snv | 2 | |||||
rs3826796 | 19 | 46296578 | upstream gene variant | G/T | snv | 7.7E-02 | 2 |